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FDA 510(k)

NATURAL LOCK ACETABULAR COMPONENT

K-Number: K830662 · 1983-04-11

Decision Date1983-04-11
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NATURAL LOCK ACETABULAR COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biosearch Assn.. It received FDA 510(k) clearance on 1983-04-11 under 510(k) number K830662. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATURAL LOCK ACETABULAR COMPONENT?

NATURAL LOCK ACETABULAR COMPONENT is a medical device that received FDA 510(k) clearance on 1983-04-11. The listed applicant is Advanced Biosearch Assn.. The 510(k) number is K830662.

When did NATURAL LOCK ACETABULAR COMPONENT receive FDA 510(k) clearance?

NATURAL LOCK ACETABULAR COMPONENT received FDA 510(k) clearance on 1983-04-11, under 510(k) number K830662.

Who is the listed applicant for NATURAL LOCK ACETABULAR COMPONENT?

The FDA 510(k) record lists Advanced Biosearch Assn. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NATURAL LOCK ACETABULAR COMPONENT?

The FDA product code for NATURAL LOCK ACETABULAR COMPONENT is JDL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Advanced Biosearch Assn. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 22 devices →

Related Devices (Code: JDL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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